A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623132



Internal ID6663300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46258921..46261224hg38UCSC Ensembl
Innerchr10:46258938..46261207hg38UCSC Ensembl
Outerchr10:46258904..46261241hg38UCSC Ensembl
chr10:47630157..47632460hg19UCSC Ensembl
Innerchr10:47630174..47632443hg19UCSC Ensembl
Outerchr10:47630140..47632477hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg382304
hg192304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13785816, essv13785817, essv13785813, essv13785815, essv13785818, essv13785814
SamplesHG02107, HG03196, HG03234, NA19474, NA18504, NA18519
Known GenesANTXRLP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623132
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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